Linked Data
gnomAD v4:
10-94988883-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94988883T>G , CM000672.2:g.94988883T>G | GRCh38 |
| NC_000010.10:g.96748640T>G , CM000672.1:g.96748640T>G | GRCh37 |
| NC_000010.9:g.96738630T>G | NCBI36 |
| NG_008385.1:g.55226T>G | |
| NG_008385.2:g.55726T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.1328T>G MANE Select | ENSP00000260682.6:p.Met443Arg | |
| ENST00000643112.1:c.*337T>G | ENSP00000496202.1:n.*337T>G | |
| ENST00000260682.6:c.1328T>G | ENSP00000260682.6:p.Met443Arg | |
| NM_000771.3:c.1328T>G | NP_000762.2:p.Met443Arg | |
| NM_000771.4:c.1328T>G MANE Select | NP_000762.2:p.Met443Arg |